Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1150753 | 0.925 | 0.120 | 6 | 32092090 | intron variant | A/G | snv | 6.3E-02 | 2 | ||
rs1748033 | 0.925 | 0.120 | 1 | 17336167 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 2 | ||
rs17581834 | 0.882 | 0.120 | 1 | 206802774 | intron variant | T/C | snv | 4.2E-02 | 3 | ||
rs1913517 | 0.925 | 0.120 | 10 | 48911009 | intron variant | A/G | snv | 0.54 | 2 | ||
rs204994 | 0.925 | 0.120 | 6 | 32187221 | non coding transcript exon variant | C/T | snv | 0.18 | 0.21 | 4 | |
rs2075876 | 0.925 | 0.120 | 21 | 44289270 | non coding transcript exon variant | G/A | snv | 0.19 | 2 | ||
rs2277798 | 0.925 | 0.120 | 21 | 42403997 | missense variant | A/G | snv | 0.55 | 0.60 | 3 | |
rs2283790 | 0.882 | 0.120 | 22 | 21602364 | intron variant | A/G | snv | 0.21 | 3 | ||
rs3117103 | 0.925 | 0.120 | 6 | 32381780 | intron variant | A/T | snv | 9.6E-02 | 2 | ||
rs340630 | 0.925 | 0.120 | 4 | 87037243 | intron variant | G/A | snv | 0.42 | 2 | ||
rs34933034 | 0.925 | 0.120 | 15 | 74787133 | intron variant | G/A;T | snv | 3 | |||
rs3890733 | 0.882 | 0.120 | 12 | 47895590 | intron variant | C/T | snv | 0.27 | 3 | ||
rs4112788 | 0.851 | 0.120 | 1 | 152578800 | downstream gene variant | A/G;T | snv | 4 | |||
rs4921283 | 0.925 | 0.120 | 5 | 160443604 | intron variant | G/A | snv | 0.52 | 2 | ||
rs4937333 | 0.882 | 0.120 | 11 | 128460625 | 3 prime UTR variant | T/C | snv | 0.45 | 4 | ||
rs494620 | 0.925 | 0.120 | 6 | 31870936 | stop gained | G/A;T | snv | 0.44; 4.1E-06 | 3 | ||
rs509749 | 0.925 | 0.120 | 1 | 160823770 | missense variant | A/G | snv | 0.54 | 0.55 | 2 | |
rs6935269 | 0.925 | 0.120 | 6 | 32292573 | intron variant | T/C | snv | 0.25 | 2 | ||
rs704853 | 0.925 | 0.120 | 1 | 167499627 | intron variant | G/T | snv | 0.15 | 2 | ||
rs708035 | 0.925 | 0.120 | 3 | 10234479 | missense variant | T/A | snv | 0.73 | 0.70 | 2 | |
rs7097397 | 0.925 | 0.120 | 10 | 48817351 | missense variant | G/A | snv | 0.38 | 0.31 | 2 | |
rs7258015 | 0.925 | 0.120 | 19 | 10338682 | missense variant | T/C | snv | 0.22 | 0.20 | 2 | |
rs771131230 | 0.925 | 0.120 | 6 | 32581827 | missense variant | C/A;T | snv | 2 | |||
rs773389640 | 0.925 | 0.120 | 6 | 32581821 | missense variant | C/G;T | snv | 2 | |||
rs906868 | 0.925 | 0.120 | 2 | 30225478 | intergenic variant | G/T | snv | 0.53 | 4 |